ENST00000405460.9:c.9101A>G
MANE Select
|
ENSP00000384582.2:p.Asp3034Gly
|
|
ENST00000639431.1:c.265+36136A>G
|
ENSP00000491057.1:n.265+36136A>G
|
|
ENST00000639473.1:n.4560A>G
|
|
|
ENST00000640012.1:c.2908A>G
|
|
|
ENST00000640374.1:n.2245A>G
|
|
|
ENST00000640779.1:c.3830A>G
|
|
|
ENST00000405460.6:c.9101A>G
|
ENSP00000384582.2:p.Asp3034Gly
|
|
ENST00000509621.1:c.1798A>G
|
|
|
NM_032119.3:c.9101A>G
|
NP_115495.3:p.Asp3034Gly
|
|
NR_003149.1:n.9114A>G
|
|
|
XM_011543675.1:c.9098A>G
|
XP_011541977.1:p.Asp3033Gly
|
|
XM_011543676.1:c.9020A>G
|
XP_011541978.1:p.Asp3007Gly
|
|
XM_011543677.1:c.6404A>G
|
XP_011541979.1:p.Asp2135Gly
|
|
XM_011543678.1:c.9101A>G
|
XP_011541980.1:p.Asp3034Gly
|
|
XM_011543679.1:c.9101A>G
|
XP_011541981.1:p.Asp3034Gly
|
|
NM_032119.4:c.9101A>G
MANE Select
|
NP_115495.3:p.Asp3034Gly
|
|
XM_017009963.2:c.9122A>G
|
XP_016865452.1:p.Asp3041Gly
|
|
XM_017009964.2:c.9119A>G
|
XP_016865453.1:p.Asp3040Gly
|
|
XM_017009965.1:c.9119A>G
|
XP_016865454.1:p.Asp3040Gly
|
|
XM_017009966.2:c.9041A>G
|
XP_016865455.1:p.Asp3014Gly
|
|
XM_017009967.1:c.9026A>G
|
XP_016865456.1:p.Asp3009Gly
|
|
XM_017009968.2:c.9122A>G
|
XP_016865457.1:p.Asp3041Gly
|
|
XM_017009969.2:c.9122A>G
|
XP_016865458.1:p.Asp3041Gly
|
|
XM_017009970.2:c.9122A>G
|
XP_016865459.1:p.Asp3041Gly
|
|
XM_017009971.2:c.9122A>G
|
XP_016865460.1:p.Asp3041Gly
|
|
XM_017009972.1:c.2240A>G
|
XP_016865461.1:p.Asp747Gly
|
|
XM_017009973.1:c.2219A>G
|
XP_016865462.1:p.Asp740Gly
|
|
XM_017009974.2:c.9122A>G
|
XP_016865463.1:p.Asp3041Gly
|
|
NR_003149.2:n.9117A>G
|
|
|